Evidence map›Paper›PMID 24700979›Full record

ArticleBulletin of the World Health Organization2014

A comparison of two visual inspection methods for cervical cancer screening among HIV-infected women in Kenya.

Megan J Huchko, Jennifer Sneden, Hannah H Leslie, Naila Abdulrahim, May Maloba, Elizabeth Bukusi, Craig R Cohen

Open access · diamondAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Bulletin of the World Health Organization, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 3 pooled it
2.4field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 3 syntheses or guidelines pooled it, 31 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Megan J HuchkoUniversity of California, San Francisco, 50 Beale Street (Suite 1200), San Francisco, CA 94105, United States of America (USA).
Jennifer SnedenUniversity of California, San Francisco, 50 Beale Street (Suite 1200), San Francisco, CA 94105, United States of America (USA).
Hannah H LeslieUniversity of California, Berkeley, USA .
Naila AbdulrahimKenya Medical Research Institute, Nairobi, Kenya .
May MalobaKenya Medical Research Institute, Nairobi, Kenya .
Elizabeth BukusiKenya Medical Research Institute, Nairobi, Kenya .
Craig R CohenUniversity of California, San Francisco, 50 Beale Street (Suite 1200), San Francisco, CA 94105, United States of America (USA).
Kenya Medical Research Institute · KEUniversity of California, Berkeley · US

Funding

Virology CoreP30AI027763 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEVEN Grant DEEKS · 1988 to 2026
$93.6M
NIAID NIH HHS P30 AI027763
6 · The paper itself

Abstract

objectiveTo determine the optimal strategy for cervical cancer screening in women with human immunodeficiency virus (HIV) infection by comparing two strategies: visual inspection of the cervix with acetic acid (VIA) and VIA followed immediately by visual inspection with Lugol's iodine (VIA/VILI) in women with a positive VIA result.

methodsData from a cervical cancer screening programme embedded in two HIV clinic sites in western Kenya were evaluated. Women at a central site underwent VIA, while women at a peripheral site underwent VIA/VILI. All women positive for cervical intraepithelial neoplasia grade 2 or worse (CIN 2+) on VIA and/or VILI had a confirmatory colposcopy, with a biopsy if necessary. Overall test positivity, positive predictive value (PPV) and the CIN 2+ detection rate were calculated for the two screening methods, with biopsy being the gold standard.

findingsBetween October 2007 and October 2010, 2338 women were screened with VIA and 1124 with VIA/VILI. In the VIA group, 26.4% of the women tested positive for CIN 2+; in the VIA/VILI group, 21.7% tested positive (P < 0.01). Histologically confirmed CIN 2+ was detected in 8.9% and 7.8% (P = 0.27) of women in the VIA and VIA/VILI groups, respectively. The PPV of VIA for biopsy-confirmed CIN 2+ in a single round of screening was 35.2%, compared with 38.2% for VIA/VILI (P = 0.41).

conclusionThe absence of any differences between VIA and VIA/VILI in detection rates or PPV for CIN 2+ suggests that VIA, an easy testing procedure, can be used alone as a cervical cancer screening strategy in low-income settings.

Indexed as

Acetic AcidAdultAge DistributionColposcopyCross-Sectional StudiesFemaleHIV InfectionsHumansIndicators and ReagentsIodidesKenyaLogistic ModelsMiddle AgedNeoplasm StagingPapanicolaou TestUterine Cervical NeoplasmsAcetic AcidIndicators and ReagentsIodidesLugol's solution

Identifiers

PMID24700979
PMCPMC3949589
OpenAlexW1975327579

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.